Step 1: Understanding sickle cell anaemia.
Sickle cell anaemia is a genetic disorder caused by a mutation in the gene coding for haemoglobin.
Step 2: Identifying the carrier genotype.
A carrier individual has one normal haemoglobin allele (Hb$^{A}$) and one sickle allele (Hb$^{S}$). Such individuals usually do not show severe symptoms.
Step 3: Conclusion.
Therefore, the genotype of a carrier individual is Hb$^{A$ Hb$^{S}$}.